Canonical Allele Identifier: CA2175494867
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48446712A= , CM000677.2:g.48446712A= GRCh38
NC_000015.9:g.48738909A= , CM000677.1:g.48738909A= GRCh37
NC_000015.8:g.46526201A= NCBI36
NG_008805.2:g.204077T= , LRG_778:g.204077T=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.5782T= ENSP00000453958.2:p.Cys1928=
ENST00000674301.2:c.5782T= ENSP00000501333.2:p.Cys1928=
ENST00000684448.1:n.4456T=
ENST00000316623.10:c.5782T= MANE Select ENSP00000325527.5:p.Cys1928=
ENST00000674301.1:c.781T= ENSP00000501333.1:p.Cys261=
ENST00000316623.9:c.5782T= ENSP00000325527.5:p.Cys1928=
ENST00000537463.6:c.*1545T= ENSP00000440294.2:n.*1545T=
ENST00000559133.5:c.1089T=
NM_000138.4:c.5782T= , LRG_778t1:c.5782T= NP_000129.3:p.Cys1928=
NM_000138.5:c.5782T= MANE Select NP_000129.3:p.Cys1928=